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Isolation and microbiological transformations of related analogues: Ulubelen, A.; Miski, M.; Mabry, T. J. J. Nat. Prod 1981, 44, 119.
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5
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0005082291
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Previous syntheses of dehydroabietic acid and its analogues: (a) Stork, G.; Schulenberg, J. W. J. Org. Chem. 1962, 84, 284-292.
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7
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0020698630
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9
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33847218271
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Recent progress in total synthesis using polyene cyclization strategy: Sakakura, A.; Ukai, A.; Ishihara, K. Nature 2007, 445, 900-903.
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Recent progress in total synthesis using polyene cyclization strategy: Sakakura, A.; Ukai, A.; Ishihara, K. Nature 2007, 445, 900-903.
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33845984909
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and early references cited therein
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(d) Uyanik, M.; Ishihara, K.; Yamamoto, H. Org. Lett. 2006, 8, 5649-5652, and early references cited therein.
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Org. Lett
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Uyanik, M.1
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0027476042
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and references therein
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Corey, E. J., Jr. J. Am. Chem. Soc. 1996, 118, 11982-11983, and references therein.
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(g) Corey, E. J., Jr. J. Am. Chem. Soc. 1996, 118, 11982-11983, and references therein.
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17
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0040340134
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(i) Bogenstätter, M.; Limberg, A.; Overman, L. E.; Tomasi, A. L. J. Am. Chem. Soc. 1999, 121, 12206-12207.
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Bogenstätter, M.1
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Tomasi, A.L.4
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18
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4344674537
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and references therein
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(j) Pattenden, G.; Gonzalez, M. A.; McCulloch, S.; Walter, A.; Woodhead, S. J. Proc. Natl. Acad. Sci. 2004, 101, 12024-12029, and references therein.
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Pattenden, G.1
Gonzalez, M.A.2
McCulloch, S.3
Walter, A.4
Woodhead, S.J.5
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20
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27244457979
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(l) Justicia, J.; Oller-Lopez, J. L.; Campaña, A. G.; Oltra, J. E.; Cuerva, J. M.; Buñuel, E.; Cardenas, D. J. J. Am. Chem. Soc. 2005, 127, 14911-14921.
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21
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0001377167
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Snider, B.B.1
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33846438613
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24
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(a) Johnson, W. S.; Elliott, J. D.; Hanson, G. J. Am. Chem. Soc. 1984, 106, 1138-1139.
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0001934843
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Mori, A.1
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27
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59849090027
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Polyene 6 was synthesized over seven steps as shown below: (Chemical Equation Presented)
-
Polyene 6 was synthesized over seven steps as shown below: (Chemical Equation Presented)
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-
-
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28
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59849084007
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Compound 7 was confirmed to be the THF formation product of 8. The formation yield of 7 was moderate partially because the minor isomer 20 was resistant to cyclization condition and could be recovered. (Chemical Equation Presented)
-
Compound 7 was confirmed to be the THF formation product of 8. The formation yield of 7 was moderate partially because the minor isomer 20 was resistant to cyclization condition and could be recovered. (Chemical Equation Presented)
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-
-
-
30
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59849091098
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The enantiomeric excess value of 4 was determined on the basis of compound 17 as shown below: (Chemical Equation Presented)
-
The enantiomeric excess value of 4 was determined on the basis of compound 17 as shown below: (Chemical Equation Presented)
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-
-
-
32
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33748664603
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(b) Bal, B. S.; Childers, W. E., Jr.; Pinnick, H. K. Tetrahedron 1981, 37, 2091-2096.
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Tetrahedron
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Bal, B.S.1
Childers Jr., W.E.2
Pinnick, H.K.3
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